TNA Facial Pain Network

Online community for patients & caregivers | 1-800-923-3608 M-F 9a-5p EST (USA)


The TNA Video Project is a collaboration between TN patients and The Facial Pain Association to raise awareness of facial pain syndromes and to celebrate the Association’s 25 years of patient support and advocacy. Join the Project and let the world hear from you, how this horrific pain can be triggered by something or some action that most people take for granted.

To view TheTNA Video Project site go to:


Latest Activity

Aidan Tavendale commented on squid's group MEN WITH TN
"accurate term really."
1 hour ago
Aidan Tavendale commented on squid's group MEN WITH TN
"Ill tell you what...neuralgia is such a very active is the other"
1 hour ago
Aidan Tavendale commented on squid's group MEN WITH TN
"Hi Squid, No reports of auriculotemporal neuralgia here. Obviously more reports of TN. No, Doctors…"
1 hour ago
Sarah Crowley is now a member of TNA Facial Pain Network
15 hours ago
squid commented on squid's group MEN WITH TN
"Hello Aiden, Welcome to the group. I see that you are having a difficult time with the issues you…"
Aidan Tavendale joined squid's group


information for men who have any form of trigeminal neuralgia or other facial pain disorders. Also…See More
Aidan Tavendale and Kat are now friends
Aidan Tavendale replied to Chris Gresham's discussion Hi my name is Chris, I have either severe nerve damage or ATN after double jaw joint replacements
"Hi Chris, Just read all your blogs...i dont even know what to comment....Ive just seperated, from…"


Motor Cortex Stimulator

Started by EdenB in Surgeries. Last reply by EdenB Jul 19. 145 Replies

Blog Posts

Anyone with Postherpetic Neuralgia?

Posted by barbara on July 20, 2016 at 10:31am 1 Comment


Posted by NC on July 17, 2016 at 7:57pm 1 Comment


Posted by Dane Proudfoot on July 12, 2016 at 10:43pm 0 Comments

ARE YOU NEW? READ THIS: Getting Started Guide


Do you have a specific topic you want to research?

Just type what you're looking for in the "search" box at the very top of the website in the blue bar, then hit the orange search button. You can search for a medication, side effect, surgery, etc. 

Search Google and the TNA Knowledge Base sites without leaving Facial Pain Network by clicking on the search options in the green bar at the bottom of the website. 

While you're here, you can:

  1. Post a question or discussion in the Forum for members to reply to.
  2. Start a blog, or read about another member's journey with facial pain.
  3. Chat with other members who are online. If you don't feel like chatting, you can click on the "green light" / gear icon at the bottom of the chat window to disconnect. 
  4. Join a group with similar interests, or create your own group.
  5. Check out support group events, or create your own event or chat date.
  6. Invite your family and friends to participate on FPN.
  7. Watch videos posted by TNA and other members about facial pain topics.

Don't forget to:

  1. Update your profile so that other members can learn about you, and upload a pic to show your personality. You can also search for other members who have something in common with you, such as the country or state you live in or your patient status. Make friends so that you can exchange private messages.
  2. Introduce yourself on the forum thread for new members.
  3. Edit your email notification settings so that FPN only sends you the amount of email you want.
  4. Update your status to let other members know what you're up to, and see all your latest activity.
  5. Help support this community by making a donation to The Facial Pain Association. Every dollar counts.
  6. Read the Terms of Use. Your participation in the TNA Facial Pain Network online community constitutes acceptance of all the conditions listed.

Questions or problems? We hope you enjoy interacting with each other, but if experience any issues, please post on the forum or send a message to the forum administrator.




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